Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
 1 
 2 
 3 
 4 
 > 
 
36 records meeting your search criteria returned- Product Code: JDR Patient Problem: Unspecified Infection Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH SPEED 13X12X12MM IMPLANT 08/22/2023
SYNTHES GMBH SPEED COMPRESSION IMPLANT KIT 13X12X12MM 08/22/2023
SYNTHES GMBH ELITE COMP IMPL KIT 15X15X15 2 LEGS 06/21/2023
SYNTHES GMBH ELITE COMP IMPL KIT 15X15X15 2 LEGS 06/21/2023
SYNTHES GMBH ELITE COMP IMPL KIT 15X15X15 2 LEGS 06/21/2023
DEPUY MITEK LLC US UNK - IMPLANT 02/16/2022
WRIGHT MEDICAL TECHNOLOGY, INC. FUSEFORCE 02/17/2021
TRIMED, INC. NITINOL STAPLE 07/10/2020
SMITH & NEPHEW, INC. TWINFIX TI 3.5 ULTRABRAID 02/03/2020
DEPUY MITEK LLC US UNKNOWN GII ANCHOR 11/04/2019
-
-